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FDA Import Refusal AEK-0117149-2/1/1 — SHANGHAI APOLO MEDICAL TECHNOLOGY CO., LTD.

SHANGHAI APOLO MEDICAL TECHNOLOGY CO., LTD. — FEI 3007120647

The FDA refused shipment AEK-0117149-2/1/1 from SHANGHAI APOLO MEDICAL TECHNOLOGY CO., LTD. (China) on June 30, 2014. The refused product falls under Devices — SYSTEM, NON-COHERENT LIGHT, PHOTODYNAMIC THERAPY. Cited charges: 118,341,508 This firm has 4 other import refusals on record.

Refusal Details

Date
June 30, 2014
Country
China
Product Category
Devices
Product Code
79MYH SYSTEM, NON-COHERENT LIGHT, PHOTODYNAMIC THERAPY
Charges
118,341,508

Recent inspections

  • 875112 (VAI Thu Mar 27 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 746517 (OAI Thu Sep 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 399-1047989-6/11/1 (Mon Sep 20 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-7659417-2/11/1 (Thu Jul 30 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-4530597-2/1/1 (Fri Mar 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 112-1220197-9/1/1 (Mon Apr 04 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources